On-Demand Solutions for Life Sciences
From Investment, Development, and Licensing Consulting to Commercialization
of Pharmaceutical, Biotech, and Medical Device Products
On-Demand Solutions for Life Sciences
From Investment, Development, and Licensing Consulting to Commercialization
of Pharmaceutical, Biotech, and Medical Device Products
Decentralized Clinical Trial (DCT) Service Using Various Mobile Web-Based Service Modules, from Participant Recruitment to Clinical Data Collection
Solutions
Maven eConsent
Maven Rscreening
Maven Rvisit
Maven RTSM
Maven Auditor+
eRecruitment Efficiently recruit protocol-compliant participants with a digital system, reducing dropout rates and saving time and costs. |
Remote Visit Utilize digital technology to conduct clinical trial visits remotely, eliminating the need for physical site visits. This approach saves time and costs for participants while enhancing participation and research quality. |
Direct to Patient Deliver investigational medicinal products (IMPs) directly to participants and reduce errors with a dashboard for immediate inventory management and delivery. Additionally, flexible integration with digital therapeutics (DTx) enables effective clinical trials. |
Blockchain Security All data stored in the Maven Service is securely managed using patented audit trail technology. This advanced blockchain-based security system protects against data manipulation and tampering, ensuring data integrity and providing verification of data authenticity. |
Decentralized Clinical Trial (DCT) Service Using Various Mobile Web-Based Service Modules, from Participant Recruitment to Clinical Data Collection
Solutions
Efficiently recruit protocol-compliant participants with a digital system, reducing dropout rates and saving time and costs.
Utilize digital technology to conduct clinical trial visits remotely, eliminating the need for physical site visits. This approach saves time and costs for participants while enhancing participation and research quality.
Deliver investigational medicinal products (IMPs) directly to participants and reduce errors with a dashboard for immediate inventory management and delivery. Additionally, flexible integration with digital therapeutics (DTx) enables effective clinical trials.
All data stored in the Maven Service is securely managed using patented audit trail technology. This advanced blockchain-based security system protects against data manipulation and tampering, ensuring data integrity and providing verification of data authenticity.
Contract Development & Commercialization Organization (CDCO) Service ranging from Product Development, Validation, Clinical Trials, Commercialization, and Post-Market Surveillance of Digital Medical Devices and Digital Therapeutics (DTx) using AI and other technologies
Solutions
Maven CDMS
Maven DCT Suite
Maven Safety
PoC and Product Development Leverage digital therapeutic algorithms and reusable software as medical device (SaMD) modules to support effective idea validation and initial product development. This accelerates the creation and transition of digital medical solutions from development to market readiness. |
Exploratory/Confirmatory Clinical Trials Enhance data management and trial operations using Maven CDMS and Maven DCT Suite. These integrated platforms allow for real-time collection, management, and analysis of clinical data, improving the accuracy and reliability of trial results and expediting the trial process. |
Product Commercialization Systematically support approvals from essential regulatory bodies such as the FDA and MFDS. Manage complex regulatory requirements to ensure regulation compliance and help products achieve a competitive edge through safe and effective market entry. |
Post-Market Surveillance Utilize Maven Safety for advanced post-launch monitoring. Detect and analyze adverse reactions promptly, report to regulatory agencies, and ensure ongoing product safety and market credibility. |
Digital-Based Full-Scope Contract Research Organization (CRO) Service combining Clinical Trial Operations and Solutions
Solutions
Maven CDMS
Maven Docs
Maven eTMF
Maven eCOA
Maven CDISC
Maven Safety
Medical Writing Provide comprehensive medical writing services for clinical trials, from designing protocols to drafting study reports, ensuring scientific accuracy and regulatory compliance. |
Project Management Comprehensive project management for effective trial design and operation, including planning and efficient patient recruitment, to ensure smooth and accurate trial execution. |
Clinical Operations Monitoring and managing all clinical trial sites, ensuring trials are conducted accurately and reliably, thereby enhancing trial credibility. |
Data Manegement Designing optimal eCRFs, reviewing and managing data entered on-site to ensure data reliability and support trial success. |
Biostatistics Setting statistical analysis methods, deriving results per the protocol, and compiling comprehensive reports and key insights. |
Pharmacovigilance Managing and reporting safety information to regulatory authorities, and analyzing all safety data to maintain research integrity and participant protection. |
Global Expansion and Licensing Strategy Support Services for Biotech and Pharmaceutical Companies
Solutions
Maven CDMS
Maven VDR
Maven Docs
Maven eTMF
Due Diligence Comprehensive due diligence services for biotech and pharmaceutical fields with a highly secure virtual data room and strict access control systems, to effectively manage investment risks and establish reliable partnerships. |
Value Evaluation Support Algorithm-based value assessments to accurately determine asset value, providing clear and substantiated information for investment decision-making. |
Deal Sourcing Conducting market research to identify potential licensing partners, developing detailed negotiation strategies, and facilitating direct contact with licensors to achieve successful licensing agreements. |
Liaison & Project Management Offering structured support throughout all business stages to help clients focus on their core operations. Utilizing our network and expertise, efficiently manage and respond to domestic and international networking on behalf of our clients. |
At JNPMEDI, we drive digital transformation in the healthcare and life sciences sectors through our expertise in cloud infrastructure management. As a certified AWS MSP Partner, we offer end-to-end services, including architecture design, implementation, management, and cost optimization.
AWS Cloud Environment Implementation We specialize in designing cloud architectures tailored to the unique needs of the life sciences industry. Our team facilitates seamless and secure migrations from on-premise systems or other cloud platforms, ensuring the establishment of reliable cloud environment. |
Cost Optimization and We provide continuous monitoring of cloud resources and implement strategic cost optimization measures, enabling our clients to operate efficiently within budget.Management |
Security and Regulatory Compliance We design and manage cloud environments that meet critical healthcare industry regulations such as GxP, HIPAA, and GDPR. This ensures secure management of sensitive medical data while maintaining full compliance with industry standards. |
Data Analytics Platform We build data analytics environments that empower our clients to derive actionable insights, supporting fast and informed decision-making processes. |
Performance Optimization and Scalability We support strategic resource scaling, allowing businesses to quickly adapt to evolving needs and workloads while ensuring efficient use of cloud resources. |
Contract Development & Commercialization Organization (CDCO) Service ranging from Product Development, Validation, Clinical Trials, Commercialization, and Post-Market Surveillance of Digital Medical Devices and Digital Therapeutics (DTx) using AI and other technologies
Solutions
Leverage digital therapeutic algorithms and reusable software as medical device (SaMD) modules to support effective idea validation and initial product development. This accelerates the creation and transition of digital medical solutions from development to market readiness.
Enhance data management and trial operations using Maven CDMS and Maven DCT Suite. These integrated platforms allow for real-time collection, management, and analysis of clinical data, improving the accuracy and reliability of trial results and expediting the trial process.
Systematically support approvals from essential regulatory bodies such as the FDA and MFDS. Manage complex regulatory requirements to ensure regulation compliance and help products achieve a competitive edge through safe and effective market entry.
Utilize Maven Safety for advanced post-launch monitoring. Detect and analyze adverse reactions promptly, report to regulatory agencies, and ensure ongoing product safety and market credibility.
Digital-Based Full-Scope Contract Research Organization (CRO) Service combining Clinical Trial Operations and Solutions
Solutions
Maven Converter
Maven Safety
Provide comprehensive medical writing services for clinical trials, from designing protocols to drafting study reports, ensuring scientific accuracy and regulatory compliance.
Comprehensive project management for effective trial design and operation, including planning and efficient patient recruitment, to ensure smooth and accurate trial execution.
Monitoring and managing all clinical trial sites, ensuring trials are conducted accurately and reliably, thereby enhancing trial credibility.
Designing optimal eCRFs, reviewing and managing data entered on-site to ensure data reliability and support trial success.
Setting statistical analysis methods, deriving results per the protocol, and compiling comprehensive reports and key insights.
Managing and reporting safety information to regulatory authorities, and analyzing all safety data to maintain research integrity and participant protection.
Global Expansion and Licensing Strategy Support Services for Biotech and Pharmaceutical Companies
Solutions
Comprehensive due diligence services for biotech and pharmaceutical fields with a highly secure virtual data room and strict access control systems, to effectively manage investment risks and establish reliable partnerships.
Algorithm-based value assessments to accurately determine asset value, providing clear and substantiated information for investment decision-making.
Conducting market research to identify potential licensing partners, developing detailed negotiation strategies, and facilitating direct contact with licensors to achieve successful licensing agreements.
Offering structured support throughout all business stages to help clients focus on their core operations. Utilizing our network and expertise, efficiently manage and respond to domestic and international networking on behalf of our clients.
At JNPMEDI, we drive digital transformation in the healthcare and life sciences sectors through our expertise in cloud infrastructure management. As a certified AWS MSP Partner, we offer end-to-end services, including architecture design, implementation, management, and cost optimization.
We specialize in designing cloud architectures tailored to the unique needs of the life sciences industry. Our team facilitates seamless and secure migrations from on-premise systems or other cloud platforms, ensuring the establishment of reliable cloud environment.
We provide continuous monitoring of cloud resources and implement strategic cost optimization measures, enabling our clients to operate efficiently within budget.
We design and manage cloud environments that meet critical healthcare industry regulations such as GxP, HIPAA, and GDPR. This ensures secure management of sensitive medical data while maintaining full compliance with industry standards.
We build data analytics environments that empower our clients to derive actionable insights, supporting fast and informed decision-making processes.
We support strategic resource scaling, allowing businesses to quickly adapt to evolving needs and workloads while ensuring efficient use of cloud resources.
